In-Depth Analysis of Genetic Variation Associated with Severe West Nile Viral Disease

por Cahill, Megan E., Loeb, Mark, Dewan, Andrew T., Montgomery, Ruth R.
Publicado 2020

dbPEC: a comprehensive literature-based database for preeclampsia related genes and phenotypes

por Uzun, Alper, Triche, Elizabeth W., Schuster, Jessica, Dewan, Andrew T., Padbury, James F.
Publicado 2016

Circulating miRNAs in the first trimester and pregnancy complications: a systematic review

por Subramanian, Anita, Weiss, Doria, Nyhan, Kate, Dewan, Andrew, Jukic, Anne Marie Z.
Publicado 2022

Targeted Sequencing and Meta-Analysis of Preterm Birth

por Uzun, Alper, Schuster, Jessica, McGonnigal, Bethany, Schorl, Christoph, Dewan, Andrew, Padbury, James
Publicado 2016

The genetic contribution of the X chromosome in age-related hearing loss

por Naderi, Elnaz, Cornejo-Sanchez, Diana M., Li, Guangyou, Schrauwen, Isabelle, Wang, Gao T., Dewan, Andrew T., Leal, Suzanne M.
Publicado 2023

Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients

por Zhao, Linlu, Triche, Elizabeth W, Walsh, Kyle M, Bracken, Michael B, Saftlas, Audrey F, Hoh, Josephine, Dewan, Andrew T
Publicado 2012

Leveraging Ethnic Group Incidence Variation to Investigate Genetic Susceptibility to Glioma: A Novel Candidate SNP Approach

por Jacobs, Daniel I., Walsh, Kyle M., Wrensch, Margaret, Wiencke, John, Jenkins, Robert, Houlston, Richard S., Bondy, Melissa, Simon, Matthias, Sanson, Marc, Gousias, Konstantinos, Schramm, Johannes, Labussière, Marianne, Di Stefano, Anna Luisa, Wichmann, H.-Erich, Müller-Nurasyid, Martina, Schreiber, Stefan, Franke, Andre, Moebus, Susanne, Eisele, Lewin, Dewan, Andrew T., Dubrow, Robert
Publicado 2012